Development and comparison of loop-mediated isothermal amplification with quantitative PCR for the specific detection of Saprolegnia spp.
Fig 4
Ten-fold dilutions of S. salmonis DNA ranging from 1 fg to 100 ng were amplified in triplicate and the reactions were repeated three times. The iTaq™ Universal SYBR® Green Supermix and qCOXF1+R1 primers were used.